Evidence map›Paper›PMID 29738844›Full record

ArticleNeuroscience letters2018

Removal of area CA3 from hippocampal slices induces postsynaptic plasticity at Schaffer collateral synapses that normalizes CA1 pyramidal cell discharge.

Theodore C Dumas, Michael R Uttaro, Carolina Barriga, Tiffany Brinkley, Maryam Halavi, Susan N Wright, Michele Ferrante, Rebekah C Evans, Sarah L Hawes, Erin M Sanders

Open access · greenAbstract read
In one paragraph

Article in Neuroscience letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 45% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Theodore C DumasKrasnow Institute for Advanced Study, United States; Psychology Department, George Mason University, Fairfax, VA 22030, United States. Electronic address: tdumas@gmu.edu.
Michael R UttaroKrasnow Institute for Advanced Study, United States.
Carolina BarrigaKrasnow Institute for Advanced Study, United States.
Tiffany BrinkleyKrasnow Institute for Advanced Study, United States.
Maryam HalaviKrasnow Institute for Advanced Study, United States.
Susan N WrightKrasnow Institute for Advanced Study, United States.
Michele FerranteKrasnow Institute for Advanced Study, United States.
Rebekah C EvansKrasnow Institute for Advanced Study, United States.
Sarah L HawesKrasnow Institute for Advanced Study, United States.
Erin M SandersKrasnow Institute for Advanced Study, United States.
Institute for Advanced Study · USGeorge Mason University · US

Funding

Postnatal functional biomarkers of hippocampal integrity in adulthood and agingR15AG045820 · NIA · GEORGE MASON UNIVERSITY · PI DUMAS, THEODORE C · 2014 to 2014
$352k
NIA NIH HHS R15 AG045820
6 · The paper itself

Abstract

Neural networks that undergo acute insults display remarkable reorganization. This injury related plasticity is thought to permit recovery of function in the face of damage that cannot be reversed. Previously, an increase in the transmission strength at Schaffer collateral to CA1 pyramidal cell synapses was observed after long-term activity reduction in organotypic hippocampal slices. Here we report that, following acute preparation of adult rat hippocampal slices and surgical removal of area CA3, input to area CA1 was reduced and Schaffer collateral synapses underwent functional strengthening. This increase in synaptic strength was limited to Schaffer collateral inputs (no alteration to temporoammonic synapses) and acted to normalize postsynaptic discharge, supporting a homeostatic or compensatory response. Short-term plasticity was not altered, but an increase in immunohistochemical labeling of GluA1 subunits was observed in the stratum radiatum (but not stratum moleculare), suggesting increased numbers of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors and a postsynaptic locus of expression. Combined, these data support the idea that, in response to the reduction in presynaptic activity caused by removal of area CA3, Schaffer collateral synapses undergo a relatively rapid increase in functional efficacy likely supported by insertion of more AMPARs, which maintains postsynaptic excitability in CA1 pyramidal neurons. This novel fast compensatory plasticity exhibits properties that would allow it to maintain optimal network activity levels in the hippocampus, a brain structure lauded for its ongoing experience-dependent malleability.

Indexed as

Excitatory Postsynaptic PotentialsNeuronal PlasticityAnimalsCA3 Region, HippocampalElectric StimulationHippocampusMalePyramidal CellsRats, Long-EvansReceptors, AMPASynapsesReceptors, AMPACA3 removalFiber volleyField excitatory postsynaptic potentialHippocampusHomeostatic synaptic plasticityPopulation spikeSchaffer collateralTemporoammonic

Identifiers

PMID29738844
PMCPMC5975193
OpenAlexW2800079182

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.